Loss of a DNA binding site within the tail of prelamin A contributes to altered heterochromatin anchorage by progerin (Q24336480)

2

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Cecilia Ostlund

3

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Howard J Worman

4

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Brigitte Buendia

5

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Isabelle Duband-Goulet

describes a project that uses

6

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language of work or name

English

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publication date

16 July 2010

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published in

FEBS Letters

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volume

584

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issue

14

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page(s)

2999-3004

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ImageQuant

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2908524/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers

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Conformation, orientation, and adsorption kinetics of dermaseptin B2 onto synthetic supports at aqueous/solid interface

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Characterization of a second highly conserved B-type lamin present in cells previously thought to contain only a single B-type lamin

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Specific and conserved sequences in D. melanogaster and C. elegans lamins and histone H2A mediate the attachment of lamins to chromosomes

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Expression and purification of recombinant human histones

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The carboxyl-terminal region common to lamins A and C contains a DNA binding domain.

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Chromatin reconstitution on small DNA rings. III. Histone H5 dependence of DNA supercoiling in the nucleosome

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inferred from PubMed ID database lookup

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based on heuristic

Identifiers

DOI

10.1016/J.FEBSLET.2010.05.032

1 reference

1725019

1725019

1 reference

1 reference

1 reference